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1 rneurons was recorded extracellularly in the urethane-anesthetized rat.
2 on two tonic indicators of REM sleep in the urethane-anesthetized rat.
3 AChRs in bladder sensory pathways in vivo in urethane anesthetized rats.
4 spiking activity in somatosensory cortex of urethane anesthetized rats.
5 on when compared to pre-infusion controls in urethane anesthetized rats.
6 f young (2-8 months) and aged (24-28 months) urethane anesthetized rats.
7 ulatory nucleus releasing norepinephrine) in urethane-anesthetized rats.
8 ield potentials (LFPs) in auditory cortex of urethane-anesthetized rats.
9 n of the NAc or mediodorsal thalamus (MD) in urethane-anesthetized rats.
10 CX in these rats and in odor-naive, control, urethane-anesthetized rats.
11 ent of LTP in area CA1 of the hippocampus of urethane-anesthetized rats.
12 igh-resolution laser Doppler (LD) imaging in urethane-anesthetized rats.
13 eminal reflex blinks and blink adaptation in urethane-anesthetized rats.
14 cturition and colorectal distention (CRD) in urethane-anesthetized rats.
15 sing extracellular single-unit recordings in urethane-anesthetized rats.
16 urinary bladder and urethra were examined in urethane-anesthetized rats.
17 n the nucleus of the solitary tract (NTS) of urethane-anesthetized rats.
18 y to the Y receptor subtypes was examined in urethane-anesthetized rats.
19 ation in spontaneously breathing vagotomized urethane-anesthetized rats.
20 ses in unanesthetized decerebrate as well as urethane-anesthetized rats.
21 gic substances into the NTS were examined in urethane-anesthetized rats.
22 ed field potentials and unitary responses in urethane-anesthetized rats.
23 nses were similar to the responses evoked in urethane-anesthetized rats.
24 ecorded in medial and lateral STN neurons of urethane-anesthetized rats.
25 leus of the amygdala was examined in fasted, urethane-anesthetized rats.
26 PL) nucleus of the thalamus were examined in urethane-anesthetized rats.
27 DPAT, into the median raphe nucleus (MRN) of urethane-anesthetized rats.
28 raction with the medial septum (MS) in male, urethane-anesthetized rats.
29 firing rate of RTN chemosensitive neurons in urethane-anesthetized rats, again independent of CO(2) l
30 eld potential recordings in cortex cultures, urethane-anesthetized rats, and awake macaque monkeys.
31 ahippocampal microinfusions of anisomycin in urethane-anesthetized rats at dosages previously used in
32 were induced pharmacologically in groups of urethane-anesthetized rats by the administration of bicu
33 ol/kg) administered intravenously (i.v. ) to urethane-anesthetized rats consistently and dose-depende
34 the ventroposterior medial thalamus (VPM) of urethane-anesthetized rats during quiescent states and d
41 rm cortex were performed in freely breathing urethane-anesthetized rats (postnatal day 7 to adult).
43 icroinjection of BMI 10 pmol into the DMH in urethane-anesthetized rats resulted in marked tachycardi
44 layer II/III neurons and field recordings in urethane-anesthetized rats stimulated with odorants.
46 ding was performed in the gracile nucleus in urethane-anesthetized rats to examine estrous variations
47 hypotension and tachycardia are elicited in urethane-anesthetized rats treated 1) with LPS (15 mg/kg
50 cally evoked spike activity was monitored in urethane-anesthetized rats using in vivo extracellular r
51 ronal basal firing profile in both nuclei of urethane-anesthetized rats using the Shannon entropy (Bi
52 stimulations of the basal forebrain (BF) in urethane-anesthetized rats, we investigated state-depend
53 ing simultaneous multisite LFP recordings in urethane-anesthetized rats, we now show that NAC DBS del